Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Antònia, Flaquer"'
Autor:
Marina Silva, Gonzalo Oteo-García, Rui Martiniano, João Guimarães, Matthew von Tersch, Ali Madour, Tarek Shoeib, Alessandro Fichera, Pierre Justeau, M. George B. Foody, Krista McGrath, Amparo Barrachina, Vicente Palomar, Katharina Dulias, Bobby Yau, Francesca Gandini, Douglas J. Clarke, Alexandra Rosa, António Brehm, Antònia Flaquer, Teresa Rito, Anna Olivieri, Alessandro Achilli, Antonio Torroni, Alberto Gómez-Carballa, Antonio Salas, Jaroslaw Bryk, Peter W. Ditchfield, Michelle Alexander, Maria Pala, Pedro A. Soares, Ceiridwen J. Edwards, Martin B. Richards
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-13 (2021)
Abstract Historical records document medieval immigration from North Africa to Iberia to create Islamic al-Andalus. Here, we present a low-coverage genome of an eleventh century CE man buried in an Islamic necropolis in Segorbe, near Valencia, Spain.
Externí odkaz:
https://doaj.org/article/4e4b92202999456fac8ec1ea96bd75dd
Autor:
Josep Pol-Fuster, Francesca Cañellas, Laura Ruiz-Guerra, Aina Medina-Dols, Bàrbara Bisbal-Carrió, Bernat Ortega-Vila, Jaume Llinàs, Jessica Hernandez-Rodriguez, Jerònia Lladó, Gabriel Olmos, Konstantin Strauch, Damià Heine-Suñer, Cristòfol Vives-Bauzà, Antònia Flaquer
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-16 (2021)
Abstract We investigated the genetic causes of major mental disorders (MMDs) including schizophrenia, bipolar disorder I, major depressive disorder and attention deficit hyperactive disorder, in a large family pedigree from Alpujarras, South of Spain
Externí odkaz:
https://doaj.org/article/604aa068781048feb2bfa2c3f746e73d
Autor:
Josep Pol-Fuster, Francesca Cañellas, Laura Ruiz-Guerra, Aina Medina-Dols, Bàrbara Bisbal-Carrió, Víctor Asensio, Bernat Ortega-Vila, Diego Marzese, Carme Vidal, Carmen Santos, Jerònia Lladó, Gabriel Olmos, Damià Heine-Suñer, Konstantin Strauch, Antònia Flaquer, Cristòfol Vives-Bauzà
Publikováno v:
Frontiers in Genetics, Vol 12 (2021)
Psychosis is a highly heritable and heterogeneous psychiatric condition. Its genetic architecture is thought to be the result of the joint effect of common and rare variants. Families with high prevalence are an interesting approach to shed light on
Externí odkaz:
https://doaj.org/article/20ce0e6571ce4dd9a2d2f3bdcbba9097
Autor:
Andreas Katsimpris, Aboulmaouahib Brahim, Wolfgang Rathmann, Anette Peters, Konstantin Strauch, Antònia Flaquer
Publikováno v:
Journal of Nutritional Science, Vol 10 (2021)
Numerous predictive models for the risk of type 2 diabetes mellitus (T2DM) exist, but a minority of them has implemented nutrition data so far, even though the significant effect of nutrition on the pathogenesis, prevention and management of T2DM has
Externí odkaz:
https://doaj.org/article/318f17ad34d34cfbacb65ee56070e8a2
Autor:
Anna Olivieri, Ali Madour, Tarek Shoeib, Martin B. Richards, João Guimarães, Marina Silva, Gonzalo Oteo-García, Pierre Justeau, Pedro Soares, António Brehm, Antònia Flaquer, Krista McGrath, Douglas J. Clarke, Antonio Torroni, Antonio Salas, Alessandro Achilli, Francesca Gandini, Peter Ditchfield, Alessandro Fichera, Alexandra Rosa, Katharina Dulias, Teresa Rito, Jarosław Bryk, Alberto Gómez-Carballa, Michelle Alexander, Bobby Yau, Amparo Barrachina, Vicente Palomar, Maria Pala, Ceiridwen J. Edwards, M. George B. Foody, Rui Martiniano, Matthew von Tersch
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-13 (2021)
Scientific Reports
Scientific Reports
Supplementary Information: The online version contains supplementary material available at https://doi.org/ 10.1038/s41598-021-95996-3.
Sequence data for UE2298/MS060 can be downloaded from the European Nucleotide Archive (accession number: PRJE
Sequence data for UE2298/MS060 can be downloaded from the European Nucleotide Archive (accession number: PRJE
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e93ce5b97a4f70d0ec9878e0750801db
Autor:
Antònia Flaquer, Susanne Rospleszcz, Eva Reischl, Sonja Zeilinger, Holger Prokisch, Thomas Meitinger, Christa Meisinger, Annette Peters, Melanie Waldenberger, Harald Grallert, Konstantin Strauch
Publikováno v:
PLoS ONE, Vol 10, Iss 5, p e0126294 (2015)
It has been suggested that mitochondrial dysfunction has an influence on lipid metabolism. The fact that mitochondrial defects can be accumulated over time as a normal part of aging may explain why cholesterol levels often are altered with age. To te
Externí odkaz:
https://doaj.org/article/b867a849259e420dab955a956e3a007e
Autor:
Antònia Flaquer, Clemens Baumbach, Jennifer Kriebel, Thomas Meitinger, Annette Peters, Melanie Waldenberger, Harald Grallert, Konstantin Strauch
Publikováno v:
PLoS ONE, Vol 9, Iss 8, p e105116 (2014)
It has been suggested that mitochondrial dysfunction plays a role in metabolic disorders including obesity, diabetes, and hypertension. The fact that mitochondrial defects can be accumulated over time as a normal part of aging may explain why some in
Externí odkaz:
https://doaj.org/article/7536084a86e9404b86d325a75fb2039e
Autor:
Rui Wang-Sattler, Hansi Weissensteiner, Peter Lichtner, Sebastian Zöllner, Christian Gieger, Antònia Flaquer, Konstantin Strauch, Karsten Suhre, Gabi Kastenmüller, Brahim Aboulmaouahib
Publikováno v:
Hum. Mol. Genet. 31, 3367-3376 (2022)
In the era of personalized medicine with more and more patient-specific targeted therapies being used, we need reliable, dynamic, faster and sensitive biomarkers both to track the causes of disease and to develop and evolve therapies during the cours
Autor:
Anette Peters, Konstantin Strauch, Antònia Flaquer, Andreas Katsimpris, Wolfgang Rathmann, Aboulmaouahib Brahim
Publikováno v:
J. Nutr. Sci. 10:e46 (2021)
Journal of Nutritional Science
Journal of Nutritional Science
Numerous predictive models for the risk of type 2 diabetes mellitus (T2DM) exist, but a minority of them has implemented nutrition data so far, even though the significant effect of nutrition on the pathogenesis, prevention and management of T2DM has
Autor:
Josep, Pol-Fuster, Francesca, Cañellas, Laura, Ruiz-Guerra, Aina, Medina-Dols, Bàrbara, Bisbal-Carrió, Víctor, Asensio, Bernat, Ortega-Vila, Diego, Marzese, Carme, Vidal, Carmen, Santos, Jerònia, Lladó, Gabriel, Olmos, Damià, Heine-Suñer, Konstantin, Strauch, Antònia, Flaquer, Cristòfol, Vives-Bauzà
Publikováno v:
Frontiers in Genetics
Psychosis is a highly heritable and heterogeneous psychiatric condition. Its genetic architecture is thought to be the result of the joint effect of common and rare variants. Families with high prevalence are an interesting approach to shed light on